Tredaniel J, Mornex F, Barillot I, Diaz O, Hennequin C, Le Pechoux C, Lavole A, Giraud P, Souquet P-J, Teixeira L, Vaylet F, Zalcman G, Baudrin L, Morin F, Milleron B
Unité de Cancérologie Thoracique, Hôpital Saint-Joseph, 185 Rue Raymond-Losserand, 75674 Paris cedex 14, France.
Rev Mal Respir. 2011 Jan;28(1):51-7. doi: 10.1016/j.rmr.2010.06.027. Epub 2011 Jan 11.
Cisplatin-based chemotherapy and concurrent radiotherapy are the standard treatments for locally advanced unresectable NSCLC. New therapeutic combinations using molecular targeted drugs are needed.
Eligible patients with previously untreated stage III non squamous, NSCLC will receive thoracic radiation (66 Gy) along with cisplatin (75 mg/m(2)) and pemetrexed (500 mg/m(2)) on day 1 administered intravenously every 21 days for four cycles; weekly cetuximab will be added from the first week of therapy. The primary objective of this phase II study (IFCT 0803) is to assess the disease control rate at the 16th week, one month after the completion of the treatment. Based on a two-stage Simon approach, a total of 106 patients are required with an interim analysis of the first 34 planned.
This trial will provide information on the feasibility, efficacy and tolerability of this new therapeutic combination. Should the primary objective be achieved, a phase III randomised study testing the position of cetuximab could be considered.
以顺铂为基础的化疗和同步放疗是局部晚期不可切除非小细胞肺癌的标准治疗方法。需要新的使用分子靶向药物的治疗组合。
符合条件的先前未接受过治疗的Ⅲ期非鳞状非小细胞肺癌患者将接受胸部放疗(66 Gy),同时在第1天静脉注射顺铂(75 mg/m²)和培美曲塞(500 mg/m²),每21天一次,共四个周期;从治疗的第一周开始每周添加西妥昔单抗。这项Ⅱ期研究(IFCT 0803)的主要目的是评估治疗完成后一个月即第16周时的疾病控制率。基于两阶段西蒙方法,共需要106例患者,对计划的前34例进行中期分析。
该试验将提供有关这种新治疗组合的可行性、疗效和耐受性的信息。如果实现了主要目标,可以考虑进行一项Ⅲ期随机研究来测试西妥昔单抗的地位。